Guest guest Posted August 16, 2004 Report Share Posted August 16, 2004 Hello All, I found your group while searching for ways to help support my daughter (Bridgette) and son-in-law (). Hope you can give some suggestions on how to be supportive to them. Logan's story: He was born on June 5th (at Camp Pendleton Military Hospital - Daddy is Lcpl in the marines) He was born with bilateral club foot, it was a shock to all. He was referred to Dr. Cassidy at San Diego Military Hospital. Received first casts on July 7th. He had the tendon snipped this past Friday August 13th. We, their whole family, live in Michigan. My husband and I were there the week he got his first casts. I know that my daughter blames herself for Logan not being " perfect " . And even tho everyone tells her it is not her fault, we have not " been there " . Logan has a big sister (Meegan). She is 2 1/2. I have tried to be as supportive as possible via long distance phone calls, but am not there for " on hand " help. Please send any suggestions that you may have. Thanks, Sally (Logan & Meegan's Grandma " Boo " ) Quote Link to comment Share on other sites More sharing options...
Guest guest Posted August 16, 2004 Report Share Posted August 16, 2004 Hi, Sally, First of all, you're a terrific grandma to take the time to try to research and seek help for your daughter & grandson! I actually received an email from Bridgette earlier this month after she read one of my posts on another board. I emailed her back but haven't heard from her again yet. I invited her to this board since we have lots of CA families here and some military families who know the ropes with Tri-care and how to deal with the system in seeking the best clubfoot care. Hopefully Bridgette will join us here soon. Hopefully by reading the various posts from the different families here, you'll know what to expect with Logan's treatment. Just understanding the different protocols and having a gut feel as to when to " tough out " difficult times during treatment versus " questioning " if something isn't right.....those are the things that a lot of moms and dads struggle with. So by educating yourself, you can help your daughter and son- in-law through the *potentially* difficult days ahead when she might call you asking advice. I had to do all that myself, but it would have been great to have another relative researching clubfoot treatment to compare notes to! There's a ton of info on this board in the files, links, and photos sections. Have you been to Dr. Ponseti's website yet? Also, here's another site geared toward internet research of the Ponseti method: http://pages.ivillage.com/ponseti_links Welcome aboard! & (3-16-00) left clubfoot, switched to Ponseti method at 4 mo. old http://ponseticlubfoot.freeservers.com/ Quote Link to comment Share on other sites More sharing options...
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